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Stability constants and formation of Cu(II) and Zn(II) phosphate minerals in the oxidized zone of base metal orebodies

Published online by Cambridge University Press:  05 July 2018

M. Clara
Affiliation:
Department of Chemistry, University of Aveiro, Aveiro, Portugal
F. Magalhães
Affiliation:
Department of Chemistry, University of Aveiro, Aveiro, Portugal
Julio Pedrosa de Jesus
Affiliation:
Department of Chemistry, University of Aveiro, Aveiro, Portugal
Peter A. Williams
Affiliation:
Department of Chemistry, University College, PO Box 78, Cardiff CF1 1XL, Wales, UK

Abstract

The free energies of formation of the minerals libethenite, Cu2PO4OH, pseudomalachite, Cu5(PO4)2(OH)4, cornetite, Cu3PO4(OH)3, tarbuttite, Zn2PO4OH, spencerite, Zn2PO4OH · 1.5H2O, and scholzite, CaZn2(PO4)2 · 2H2O, have been determined at 298.2 K using solution techniques. The values of ΔfG° (298.2 K) for the above minerals are, respectively, −1228.8±3.0, −2840.3±4.2, −1600.9±5.9, −1632.1±4.0, −1982.4±3.1, and −3556.7±7.6 kJ mol−1. These results, together with others from the literature concerning hopeite, Zn3(PO4)2·4H2O, hydroxyapatite, Ca5(PO4)3(OH), and the synthetic salt Cu3(PO4)2 · 2H2O have been used to construct a model for the formation of suites of Zn(II) and Cu(II) phosphate minerals found in the oxidation zone of base metal orebodies. The distributions and modes of occurrence of many natural assemblages of these minerals are readily explained by the model. Particular attention has been focused on deposits at Broken Hill, Zambia, and Saginaw Hill, Arizona, USA.

Type
Mineral Chemistry
Copyright
Copyright © The Mineralogical Society of Great Britain and Ireland 1986

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Footnotes

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Author for correspondence

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